Canonical Allele Identifier: CA495902956

Gene: TK2

Linked Data

• MyVariant Identifiers: chr16:g.66547661G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66513758G>A , CM000678.2:g.66513758G>A	GRCh38
NC_000016.9:g.66547661G>A , CM000678.1:g.66547661G>A	GRCh37
NC_000016.8:g.65105162G>A	NCBI36
NG_016862.1:g.41655C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299697.12:c.504C>T	ENSP00000299697.9:p.Ser168=
ENST00000417693.8:c.618C>T	ENSP00000407469.5:p.Ser206=
ENST00000451102.7:c.579C>T	ENSP00000414334.4:p.Ser193=
ENST00000527284.6:c.563-1692C>T
ENST00000527800.6:c.381C>T	ENSP00000433770.1:p.Ser127=
ENST00000544898.6:c.672C>T MANE Select	ENSP00000440898.2:p.Ser224=
ENST00000567357.6:c.*530C>T	ENSP00000457959.2:n.*530C>T
ENST00000569718.6:c.410C>T	ENSP00000464313.2:p.Ala137Val
ENST00000620035.5:c.428C>T	ENSP00000483833.2:p.Ala143Val
ENST00000676538.1:c.255C>T
ENST00000676904.1:c.143C>T
ENST00000677296.1:n.54C>T
ENST00000677379.1:c.313C>T	ENSP00000503672.1:n.313C>T
ENST00000677420.1:c.381C>T	ENSP00000504648.1:p.Ser127=
ENST00000677555.1:c.381C>T	ENSP00000503331.1:p.Ser127=
ENST00000677715.1:c.381C>T	ENSP00000502950.1:p.Ser127=
ENST00000677753.1:n.54C>T
ENST00000677961.1:n.84C>T
ENST00000678015.1:c.381C>T	ENSP00000502959.1:p.Ser127=
ENST00000678190.1:c.54C>T	ENSP00000503824.1:p.Ser18=
ENST00000678282.1:n.54C>T
ENST00000678297.1:c.381C>T	ENSP00000503472.1:p.Ser127=
ENST00000299697.11:c.672C>T	ENSP00000299697.8:p.Ser224=
ENST00000417693.7:c.744C>T	ENSP00000407469.4:p.Ser248=
ENST00000451102.6:c.798C>T	ENSP00000414334.3:p.Ser266=
ENST00000525974.5:c.381C>T	ENSP00000434594.1:p.Ser127=
ENST00000527284.5:c.579C>T	ENSP00000435312.1:p.Ser193=
ENST00000527800.5:c.381C>T	ENSP00000433770.1:p.Ser127=
ENST00000544898.5:c.672C>T	ENSP00000440898.2:p.Ser224=
ENST00000545043.6:c.597C>T	ENSP00000438143.2:p.Ser199=
ENST00000561527.5:n.231C>T
ENST00000561728.1:c.121C>T
ENST00000561905.2:c.26C>T
ENST00000562552.5:n.488C>T
ENST00000563099.5:n.199C>T
ENST00000563369.6:c.381C>T	ENSP00000463560.1:p.Ser127=
ENST00000563478.5:c.381C>T	ENSP00000462341.1:p.Ser127=
ENST00000564792.1:n.327C>T
ENST00000564917.5:c.723C>T	ENSP00000455187.1:p.Ser241=
ENST00000567357.5:c.*530C>T	ENSP00000457959.1:n.*530C>T
ENST00000569718.5:c.397C>T
ENST00000620035.4:c.618C>T	ENSP00000483833.1:p.Ser206=
NM_001172643.1:c.579C>T	NP_001166114.1:p.Ser193=
NM_001172644.1:c.597C>T	NP_001166115.1:p.Ser199=
NM_001172645.1:c.618C>T	NP_001166116.1:p.Ser206=
NM_001271934.1:c.525C>T	NP_001258863.1:p.Ser175=
NM_001271935.1:c.410C>T	NP_001258864.1:p.Ala137Val
NM_001272050.1:c.381C>T	NP_001258979.1:p.Ser127=
NM_004614.4:c.672C>T	NP_004605.4:p.Ser224=
NR_073520.1:n.1951C>T
NM_001172644.2:c.597C>T	NP_001166115.1:p.Ser199=
NM_001271934.2:c.525C>T	NP_001258863.1:p.Ser175=
NM_001272050.2:c.381C>T	NP_001258979.1:p.Ser127=
NM_004614.5:c.672C>T MANE Select	NP_004605.4:p.Ser224=
NR_073520.2:n.1661C>T
NM_001172645.2:c.618C>T	NP_001166116.1:p.Ser206=